CA2320180C - Derives de cyclohexanediol - Google Patents
Derives de cyclohexanediol Download PDFInfo
- Publication number
- CA2320180C CA2320180C CA002320180A CA2320180A CA2320180C CA 2320180 C CA2320180 C CA 2320180C CA 002320180 A CA002320180 A CA 002320180A CA 2320180 A CA2320180 A CA 2320180A CA 2320180 C CA2320180 C CA 2320180C
- Authority
- CA
- Canada
- Prior art keywords
- hydroxy
- dimethyl
- cyclohexane
- diol
- trifluoromethyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
- 150000001875 compounds Chemical class 0.000 claims abstract description 118
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 21
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims abstract description 14
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 12
- 208000035475 disorder Diseases 0.000 claims abstract description 10
- 208000017520 skin disease Diseases 0.000 claims abstract description 10
- 230000003463 hyperproliferative effect Effects 0.000 claims abstract description 9
- 230000002265 prevention Effects 0.000 claims abstract description 8
- 201000004681 Psoriasis Diseases 0.000 claims abstract description 7
- 206010004146 Basal cell carcinoma Diseases 0.000 claims abstract description 6
- 206010020649 Hyperkeratosis Diseases 0.000 claims abstract description 6
- 208000001126 Keratosis Diseases 0.000 claims abstract description 6
- 230000008832 photodamage Effects 0.000 claims abstract description 6
- 229910052731 fluorine Inorganic materials 0.000 claims abstract description 4
- 239000011737 fluorine Substances 0.000 claims abstract description 4
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 4
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims abstract description 3
- 239000001257 hydrogen Substances 0.000 claims abstract description 3
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims abstract description 3
- 125000005010 perfluoroalkyl group Chemical group 0.000 claims abstract description 3
- 239000008194 pharmaceutical composition Substances 0.000 claims description 7
- 125000006239 protecting group Chemical group 0.000 claims description 7
- FPGGTKZVZWFYPV-UHFFFAOYSA-M tetrabutylammonium fluoride Chemical compound [F-].CCCC[N+](CCCC)(CCCC)CCCC FPGGTKZVZWFYPV-UHFFFAOYSA-M 0.000 claims description 6
- PKGBMNJPRJDFJA-KROAHAAKSA-N (1r,3r)-5-[(2e,9z)-12,12,12-trifluoro-11-hydroxy-7,7-dimethyl-11-(trifluoromethyl)dodeca-2,9-dienylidene]cyclohexane-1,3-diol Chemical compound FC(F)(F)C(O)(C(F)(F)F)\C=C/CC(C)(C)CCC\C=C\C=C1C[C@@H](O)C[C@H](O)C1 PKGBMNJPRJDFJA-KROAHAAKSA-N 0.000 claims description 5
- 239000004480 active ingredient Substances 0.000 claims description 4
- 239000003937 drug carrier Substances 0.000 claims description 4
- PKGBMNJPRJDFJA-ILOVMYOISA-N (1r,3r)-5-[(2e,9e)-12,12,12-trifluoro-11-hydroxy-7,7-dimethyl-11-(trifluoromethyl)dodeca-2,9-dienylidene]cyclohexane-1,3-diol Chemical compound FC(F)(F)C(O)(C(F)(F)F)/C=C/CC(C)(C)CCC\C=C\C=C1C[C@@H](O)C[C@H](O)C1 PKGBMNJPRJDFJA-ILOVMYOISA-N 0.000 claims description 3
- JEPRGZHDISKAFV-VRKMBTERSA-N (1r,3r)-5-[(e)-11-hydroxy-7,7,11-trimethyldodec-2-enylidene]cyclohexane-1,3-diol Chemical compound CC(C)(O)CCCC(C)(C)CCC\C=C\C=C1C[C@@H](O)C[C@H](O)C1 JEPRGZHDISKAFV-VRKMBTERSA-N 0.000 claims description 3
- XCKDKBYJISIVLS-UJDIOAMCSA-N (1r,3s,5z)-4-methylidene-5-[(2e,9e)-12,12,12-trifluoro-11-hydroxy-7,7-dimethyl-11-(trifluoromethyl)dodeca-2,9-dienylidene]cyclohexane-1,3-diol Chemical compound FC(F)(F)C(O)(C(F)(F)F)/C=C/CC(C)(C)CCC\C=C\C=C1\C[C@@H](O)C[C@H](O)C1=C XCKDKBYJISIVLS-UJDIOAMCSA-N 0.000 claims description 3
- IBHTYSPIJQFKQT-VWCSXSMNSA-N (1r,3s,5z)-5-[(e)-11-hydroxy-7,7,11-trimethyldodec-2-enylidene]-4-methylidenecyclohexane-1,3-diol Chemical compound CC(C)(O)CCCC(C)(C)CCC\C=C\C=C1\C[C@@H](O)C[C@H](O)C1=C IBHTYSPIJQFKQT-VWCSXSMNSA-N 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 3
- NWGZNUOCKYVHQD-ZTWZVARISA-N (1r,3r)-5-[(2e,9e)-11-hydroxy-7,7,11-trimethyldodeca-2,9-dienylidene]cyclohexane-1,3-diol Chemical compound CC(O)(C)/C=C/CC(C)(C)CCC\C=C\C=C1C[C@@H](O)C[C@H](O)C1 NWGZNUOCKYVHQD-ZTWZVARISA-N 0.000 claims description 2
- 239000012442 inert solvent Substances 0.000 claims description 2
- 208000029443 keratinization disease Diseases 0.000 claims 3
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 claims 2
- AZVMIDNMKFAJAG-VRKMBTERSA-N (1r,3r)-5-[(e)-11-hydroxy-7,7,11-trimethyldodec-2-en-9-ynylidene]cyclohexane-1,3-diol Chemical compound CC(O)(C)C#CCC(C)(C)CCC\C=C\C=C1C[C@@H](O)C[C@H](O)C1 AZVMIDNMKFAJAG-VRKMBTERSA-N 0.000 claims 1
- XTTAZBGJFAPIOL-QZJSNOFBSA-N (1r,3r)-5-[(e)-12,12,12-trifluoro-11-hydroxy-7,7-dimethyl-11-(trifluoromethyl)dodec-2-enylidene]cyclohexane-1,3-diol Chemical compound FC(F)(F)C(O)(C(F)(F)F)CCCC(C)(C)CCC\C=C\C=C1C[C@@H](O)C[C@H](O)C1 XTTAZBGJFAPIOL-QZJSNOFBSA-N 0.000 claims 1
- XCKDKBYJISIVLS-LFTBMKPKSA-N (1r,3s,5z)-4-methylidene-5-[(2e,9z)-12,12,12-trifluoro-11-hydroxy-7,7-dimethyl-11-(trifluoromethyl)dodeca-2,9-dienylidene]cyclohexane-1,3-diol Chemical compound FC(F)(F)C(O)(C(F)(F)F)\C=C/CC(C)(C)CCC\C=C\C=C1\C[C@@H](O)C[C@H](O)C1=C XCKDKBYJISIVLS-LFTBMKPKSA-N 0.000 claims 1
- MPBBMXDYNMLSLM-VUIHPWRZSA-N (1r,3s,5z)-4-methylidene-5-[(e)-12,12,12-trifluoro-11-hydroxy-7,7-dimethyl-11-(trifluoromethyl)dodec-2-enylidene]cyclohexane-1,3-diol Chemical compound FC(F)(F)C(O)(C(F)(F)F)CCCC(C)(C)CCC\C=C\C=C1\C[C@@H](O)C[C@H](O)C1=C MPBBMXDYNMLSLM-VUIHPWRZSA-N 0.000 claims 1
- NVBSXCPICFBCAY-ARPRRWEESA-N (1s,3z)-3-[(2e,9e)-11-hydroxy-7,7,11-trimethyldodeca-2,9-dienylidene]-4-methylidenecyclohexan-1-ol Chemical compound CC(C)(O)\C=C\CC(C)(C)CCC\C=C\C=C1\C[C@@H](O)CCC1=C NVBSXCPICFBCAY-ARPRRWEESA-N 0.000 claims 1
- DRDFFFVMRIMFTH-YTSQDVJWSA-N (1s,3z)-3-[(e)-11-hydroxy-7,7,11-trimethyldodec-2-en-9-ynylidene]-4-methylidenecyclohexan-1-ol Chemical compound CC(O)(C)C#CCC(C)(C)CCC\C=C\C=C1\C[C@@H](O)CCC1=C DRDFFFVMRIMFTH-YTSQDVJWSA-N 0.000 claims 1
- FFLVDVFJXUYBMV-YTSQDVJWSA-N (1s,3z)-3-[(e)-11-hydroxy-7,7,11-trimethyldodec-2-enylidene]-4-methylidenecyclohexan-1-ol Chemical compound CC(C)(O)CCCC(C)(C)CCC\C=C\C=C1\C[C@@H](O)CCC1=C FFLVDVFJXUYBMV-YTSQDVJWSA-N 0.000 claims 1
- 230000003780 keratinization Effects 0.000 abstract description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 186
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 186
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 79
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 76
- 229940093499 ethyl acetate Drugs 0.000 description 62
- 235000019439 ethyl acetate Nutrition 0.000 description 62
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 61
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 61
- 238000003818 flash chromatography Methods 0.000 description 51
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 47
- 239000003921 oil Substances 0.000 description 47
- 235000019198 oils Nutrition 0.000 description 47
- 229910052938 sodium sulfate Inorganic materials 0.000 description 47
- 235000011152 sodium sulphate Nutrition 0.000 description 47
- 239000002904 solvent Substances 0.000 description 40
- 239000000243 solution Substances 0.000 description 38
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 32
- 239000011541 reaction mixture Substances 0.000 description 26
- 239000000203 mixture Substances 0.000 description 24
- MZRVEZGGRBJDDB-UHFFFAOYSA-N N-Butyllithium Chemical compound [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 description 22
- 238000003756 stirring Methods 0.000 description 19
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 18
- 239000012267 brine Substances 0.000 description 18
- 238000001704 evaporation Methods 0.000 description 18
- 230000008020 evaporation Effects 0.000 description 18
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 18
- 238000002360 preparation method Methods 0.000 description 18
- 239000000047 product Substances 0.000 description 18
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 18
- 238000001035 drying Methods 0.000 description 16
- VEPTXBCIDSFGBF-UHFFFAOYSA-M tetrabutylazanium;fluoride;trihydrate Chemical compound O.O.O.[F-].CCCC[N+](CCCC)(CCCC)CCCC VEPTXBCIDSFGBF-UHFFFAOYSA-M 0.000 description 16
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 14
- 239000012043 crude product Substances 0.000 description 14
- 238000000605 extraction Methods 0.000 description 14
- 238000005406 washing Methods 0.000 description 14
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 12
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 12
- 238000006243 chemical reaction Methods 0.000 description 12
- 235000020964 calcitriol Nutrition 0.000 description 11
- 239000011612 calcitriol Substances 0.000 description 11
- GMRQFYUYWCNGIN-NKMMMXOESA-N calcitriol Chemical compound C1(/[C@@H]2CC[C@@H]([C@]2(CCC1)C)[C@@H](CCCC(C)(C)O)C)=C\C=C1\C[C@@H](O)C[C@H](O)C1=C GMRQFYUYWCNGIN-NKMMMXOESA-N 0.000 description 11
- 229960005084 calcitriol Drugs 0.000 description 11
- -1 tert.-butyl Chemical group 0.000 description 11
- 150000001299 aldehydes Chemical class 0.000 description 10
- 238000001914 filtration Methods 0.000 description 9
- 239000000543 intermediate Substances 0.000 description 9
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 8
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 8
- 239000012230 colorless oil Substances 0.000 description 8
- 238000010791 quenching Methods 0.000 description 8
- 230000000171 quenching effect Effects 0.000 description 8
- MCSXGCZMEPXKIW-UHFFFAOYSA-N 3-hydroxy-4-[(4-methyl-2-nitrophenyl)diazenyl]-N-(3-nitrophenyl)naphthalene-2-carboxamide Chemical compound Cc1ccc(N=Nc2c(O)c(cc3ccccc23)C(=O)Nc2cccc(c2)[N+]([O-])=O)c(c1)[N+]([O-])=O MCSXGCZMEPXKIW-UHFFFAOYSA-N 0.000 description 7
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- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 6
- 241000699670 Mus sp. Species 0.000 description 6
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 6
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- 150000002009 diols Chemical class 0.000 description 6
- 238000004128 high performance liquid chromatography Methods 0.000 description 6
- RCBVKBFIWMOMHF-UHFFFAOYSA-L hydroxy-(hydroxy(dioxo)chromio)oxy-dioxochromium;pyridine Chemical compound C1=CC=NC=C1.C1=CC=NC=C1.O[Cr](=O)(=O)O[Cr](O)(=O)=O RCBVKBFIWMOMHF-UHFFFAOYSA-L 0.000 description 6
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- 239000007858 starting material Substances 0.000 description 6
- 238000012360 testing method Methods 0.000 description 6
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- RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 description 6
- 150000003710 vitamin D derivatives Chemical class 0.000 description 6
- VRTMGTJIPBGYBB-UHFFFAOYSA-N 5,5,9-trimethyldec-7-yne-1,9-diol Chemical compound OCCCCC(C)(C)CC#CC(C)(C)O VRTMGTJIPBGYBB-UHFFFAOYSA-N 0.000 description 5
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- 229930003316 Vitamin D Natural products 0.000 description 5
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- ZDYVRSLAEXCVBX-UHFFFAOYSA-N pyridinium p-toluenesulfonate Chemical compound C1=CC=[NH+]C=C1.CC1=CC=C(S([O-])(=O)=O)C=C1 ZDYVRSLAEXCVBX-UHFFFAOYSA-N 0.000 description 5
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- 229940046008 vitamin d Drugs 0.000 description 5
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- PAAWYMXERVZEDS-YVMONPNESA-N (z)-10,10,10-trifluoro-5,5-dimethyl-9-(trifluoromethyl)dec-7-ene-1,9-diol Chemical compound OCCCCC(C)(C)C\C=C/C(O)(C(F)(F)F)C(F)(F)F PAAWYMXERVZEDS-YVMONPNESA-N 0.000 description 2
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- SLZVEFGBTWSRMN-UHFFFAOYSA-N ethyl 7-hydroxy-5,5-dimethylhept-2-enoate Chemical compound CCOC(=O)C=CCC(C)(C)CCO SLZVEFGBTWSRMN-UHFFFAOYSA-N 0.000 description 1
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- 102000051544 human VDR Human genes 0.000 description 1
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- XMGQYMWWDOXHJM-UHFFFAOYSA-N limonene Chemical compound CC(=C)C1CCC(C)=CC1 XMGQYMWWDOXHJM-UHFFFAOYSA-N 0.000 description 1
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- 239000004292 methyl p-hydroxybenzoate Substances 0.000 description 1
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- LSEFCHWGJNHZNT-UHFFFAOYSA-M methyl(triphenyl)phosphanium;bromide Chemical compound [Br-].C=1C=CC=CC=1[P+](C=1C=CC=CC=1)(C)C1=CC=CC=C1 LSEFCHWGJNHZNT-UHFFFAOYSA-M 0.000 description 1
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- 125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000005935 nucleophilic addition reaction Methods 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
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- 125000001181 organosilyl group Chemical group [SiH3]* 0.000 description 1
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- AUONHKJOIZSQGR-UHFFFAOYSA-N oxophosphane Chemical compound P=O AUONHKJOIZSQGR-UHFFFAOYSA-N 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 125000006340 pentafluoro ethyl group Chemical group FC(F)(F)C(F)(F)* 0.000 description 1
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- 239000000546 pharmaceutical excipient Substances 0.000 description 1
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- 238000013310 pig model Methods 0.000 description 1
- 229920000059 polyethylene glycol stearate Polymers 0.000 description 1
- 229940068917 polyethylene glycols Drugs 0.000 description 1
- 239000001818 polyoxyethylene sorbitan monostearate Substances 0.000 description 1
- 235000010989 polyoxyethylene sorbitan monostearate Nutrition 0.000 description 1
- 229940113124 polysorbate 60 Drugs 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 229920001592 potato starch Polymers 0.000 description 1
- 230000003389 potentiating effect Effects 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
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- 150000003138 primary alcohols Chemical class 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 230000002062 proliferating effect Effects 0.000 description 1
- 230000035755 proliferation Effects 0.000 description 1
- 239000004405 propyl p-hydroxybenzoate Substances 0.000 description 1
- 229960003415 propylparaben Drugs 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- CVHZOJJKTDOEJC-UHFFFAOYSA-N saccharin Chemical compound C1=CC=C2C(=O)NS(=O)(=O)C2=C1 CVHZOJJKTDOEJC-UHFFFAOYSA-N 0.000 description 1
- 229940081974 saccharin Drugs 0.000 description 1
- 235000019204 saccharin Nutrition 0.000 description 1
- 239000000901 saccharin and its Na,K and Ca salt Substances 0.000 description 1
- 210000001732 sebaceous gland Anatomy 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000004208 shellac Substances 0.000 description 1
- 229940113147 shellac Drugs 0.000 description 1
- ZLGIYFNHBLSMPS-ATJNOEHPSA-N shellac Chemical compound OCCCCCC(O)C(O)CCCCCCCC(O)=O.C1C23[C@H](C(O)=O)CCC2[C@](C)(CO)[C@@H]1C(C(O)=O)=C[C@@H]3O ZLGIYFNHBLSMPS-ATJNOEHPSA-N 0.000 description 1
- 235000013874 shellac Nutrition 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000004334 sorbic acid Substances 0.000 description 1
- 239000001587 sorbitan monostearate Substances 0.000 description 1
- 235000011076 sorbitan monostearate Nutrition 0.000 description 1
- 229940035048 sorbitan monostearate Drugs 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 230000036561 sun exposure Effects 0.000 description 1
- 239000000375 suspending agent Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 239000003765 sweetening agent Substances 0.000 description 1
- 239000006188 syrup Substances 0.000 description 1
- 235000020357 syrup Nutrition 0.000 description 1
- MDDUHVRJJAFRAU-UPFOFRTLSA-N tert-butyl-[(1s,3z)-5-[tert-butyl(dimethyl)silyl]oxy-3-(2-diphenylphosphorylethylidene)-2-methylidenecyclohexyl]oxy-dimethylsilane Chemical compound C1C(O[Si](C)(C)C(C)(C)C)C[C@H](O[Si](C)(C)C(C)(C)C)C(=C)\C1=C/CP(=O)(C=1C=CC=CC=1)C1=CC=CC=C1 MDDUHVRJJAFRAU-UPFOFRTLSA-N 0.000 description 1
- SHONZQYRKMHEFV-UHFFFAOYSA-N tert-butyl-[3,3-dimethyl-7-(oxan-2-yloxy)heptoxy]-dimethylsilane Chemical compound CC(C)(C)[Si](C)(C)OCCC(C)(C)CCCCOC1CCCCO1 SHONZQYRKMHEFV-UHFFFAOYSA-N 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 125000001412 tetrahydropyranyl group Chemical group 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- 231100001274 therapeutic index Toxicity 0.000 description 1
- 229940100611 topical cream Drugs 0.000 description 1
- 229940100615 topical ointment Drugs 0.000 description 1
- 239000012049 topical pharmaceutical composition Substances 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 238000013518 transcription Methods 0.000 description 1
- 230000035897 transcription Effects 0.000 description 1
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- IIHPVYJPDKJYOU-UHFFFAOYSA-N triphenylcarbethoxymethylenephosphorane Chemical compound C=1C=CC=CC=1P(C=1C=CC=CC=1)(=CC(=O)OCC)C1=CC=CC=C1 IIHPVYJPDKJYOU-UHFFFAOYSA-N 0.000 description 1
- FIQMHBFVRAXMOP-UHFFFAOYSA-N triphenylphosphane oxide Chemical compound C=1C=CC=CC=1P(C=1C=CC=CC=1)(=O)C1=CC=CC=C1 FIQMHBFVRAXMOP-UHFFFAOYSA-N 0.000 description 1
- 125000002948 undecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000002966 varnish Substances 0.000 description 1
- 230000004584 weight gain Effects 0.000 description 1
- 235000019786 weight gain Nutrition 0.000 description 1
- 239000009637 wintergreen oil Substances 0.000 description 1
- 238000010626 work up procedure Methods 0.000 description 1
- GVJHHUAWPYXKBD-IEOSBIPESA-N α-tocopherol Chemical compound OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-IEOSBIPESA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/06—Antipsoriatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C403/00—Derivatives of cyclohexane or of a cyclohexene or of cyclohexadiene, having a side-chain containing an acyclic unsaturated part of at least four carbon atoms, this part being directly attached to the cyclohexane or cyclohexene or cyclohexadiene rings, e.g. vitamin A, beta-carotene, beta-ionone
- C07C403/06—Derivatives of cyclohexane or of a cyclohexene or of cyclohexadiene, having a side-chain containing an acyclic unsaturated part of at least four carbon atoms, this part being directly attached to the cyclohexane or cyclohexene or cyclohexadiene rings, e.g. vitamin A, beta-carotene, beta-ionone having side-chains substituted by singly-bound oxygen atoms
- C07C403/08—Derivatives of cyclohexane or of a cyclohexene or of cyclohexadiene, having a side-chain containing an acyclic unsaturated part of at least four carbon atoms, this part being directly attached to the cyclohexane or cyclohexene or cyclohexadiene rings, e.g. vitamin A, beta-carotene, beta-ionone having side-chains substituted by singly-bound oxygen atoms by hydroxy groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/27—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation
- C07C45/29—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation of hydroxy groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/27—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation
- C07C45/29—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation of hydroxy groups
- C07C45/292—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation of hydroxy groups with chromium derivatives
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C47/00—Compounds having —CHO groups
- C07C47/02—Saturated compounds having —CHO groups bound to acyclic carbon atoms or to hydrogen
- C07C47/19—Saturated compounds having —CHO groups bound to acyclic carbon atoms or to hydrogen containing hydroxy groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C47/00—Compounds having —CHO groups
- C07C47/20—Unsaturated compounds having —CHO groups bound to acyclic carbon atoms
- C07C47/26—Unsaturated compounds having —CHO groups bound to acyclic carbon atoms containing hydroxy groups
- C07C47/263—Unsaturated compounds having —CHO groups bound to acyclic carbon atoms containing hydroxy groups acyclic
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C47/00—Compounds having —CHO groups
- C07C47/20—Unsaturated compounds having —CHO groups bound to acyclic carbon atoms
- C07C47/26—Unsaturated compounds having —CHO groups bound to acyclic carbon atoms containing hydroxy groups
- C07C47/273—Unsaturated compounds having —CHO groups bound to acyclic carbon atoms containing hydroxy groups containing halogen
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/18—Compounds having one or more C—Si linkages as well as one or more C—O—Si linkages
- C07F7/1804—Compounds having Si-O-C linkages
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/07—Optical isomers
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/09—Geometrical isomers
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/12—Systems containing only non-condensed rings with a six-membered ring
- C07C2601/14—The ring being saturated
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Dermatology (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Les composés de la formule (I), dans laquelle X représente C=CH2 ou CH2; Y et Z représentent indépendamment l'un de l'autre hydrogène, fluor ou hydroxy, A représente -CC-, -CH=CH- ou -CH2-CH2, R<1> et R<2> représentent indépendamment l'un de l'autre alkyle ou perfluoroalkyle, et R<3> représente alkyle inférieur, sont utiles dans le traitement ou dans la prévention de maladies hyperprolifératives de la peau, notamment du psoriasis, des carcinomes basocellulaires, des troubles de la kératinisation et la kératose, ou pour s'opposer aux états associés à une photoaltération.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP98103346.7 | 1998-02-26 | ||
EP98103346 | 1998-02-26 | ||
PCT/EP1999/001118 WO1999043646A1 (fr) | 1998-02-26 | 1999-02-20 | Derives de cyclohexanediol |
Publications (2)
Publication Number | Publication Date |
---|---|
CA2320180A1 CA2320180A1 (fr) | 1999-09-02 |
CA2320180C true CA2320180C (fr) | 2005-06-07 |
Family
ID=8231480
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA002320180A Expired - Fee Related CA2320180C (fr) | 1998-02-26 | 1999-02-20 | Derives de cyclohexanediol |
Country Status (21)
Country | Link |
---|---|
US (1) | US6184422B1 (fr) |
EP (1) | EP1056716B1 (fr) |
JP (1) | JP3507435B2 (fr) |
KR (1) | KR20010041313A (fr) |
CN (1) | CN1133621C (fr) |
AR (1) | AR018120A1 (fr) |
AT (1) | ATE229503T1 (fr) |
AU (1) | AU751241B2 (fr) |
BR (1) | BR9908315A (fr) |
CA (1) | CA2320180C (fr) |
CO (1) | CO4980898A1 (fr) |
DE (1) | DE69904442T2 (fr) |
DK (1) | DK1056716T3 (fr) |
ES (1) | ES2188134T3 (fr) |
MA (1) | MA26609A1 (fr) |
MY (1) | MY133520A (fr) |
PE (1) | PE20000267A1 (fr) |
PT (1) | PT1056716E (fr) |
TR (1) | TR200002477T2 (fr) |
WO (1) | WO1999043646A1 (fr) |
ZA (1) | ZA991550B (fr) |
Families Citing this family (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2000059855A1 (fr) * | 1999-04-01 | 2000-10-12 | Esperion Therapeutics, Inc. | Composes d'ether, compositions et leurs utilisations |
EP1094060B1 (fr) * | 1999-10-18 | 2004-04-28 | Basilea Pharmaceutica AG | Procédé pour la préparation de dérivés de rétiférol |
US6310262B1 (en) * | 1999-10-18 | 2001-10-30 | Basilea Pharmaceutica Ag | Process for preparing retiferol derivatives |
MXPA03004074A (es) * | 2000-11-22 | 2003-09-04 | Hoffmann La Roche | Derivados de retiferol y su uso en el tratamiento de enfermedades o trastornos de la piel asociadas con fotoda°o. |
EP1466900B1 (fr) * | 2001-12-26 | 2009-01-14 | Hiroaki Takayama | Derives de la vitamine d-double substitution |
US6723755B2 (en) | 2002-06-12 | 2004-04-20 | Piotr Chomczynski | Method of treating rosacea |
US7812057B2 (en) * | 2004-08-25 | 2010-10-12 | Molecular Research Center, Inc. | Cosmetic compositions |
ES2533719T3 (es) * | 2005-08-30 | 2015-04-14 | Wisconsin Alumni Research Foundation | Análogos Des-C,D de 1alfa,25-dihidroxi-19-norvitamina D3 |
GB0712653D0 (en) | 2007-06-28 | 2007-08-08 | Syngenta Ltd | Novel herbicides |
CA2712748A1 (fr) * | 2008-01-22 | 2009-07-30 | Wisconsin Alumni Reasearch Foundation | Analogues 13,13-dimethyl-des-c,d de composes de 1a, 25-dihydroxy-19-nor-vitamine d3 et formes posologiques de compositions topiques et procedes de traitement d'etats pathologiques |
MX339746B (es) | 2009-01-27 | 2016-06-08 | Berg Llc | Vitamina d3 y análogos de la misma para aliviar efectos secundarios asociados con la quimioterapia. |
JP5978130B2 (ja) | 2009-08-14 | 2016-08-24 | バーグ エルエルシー | 脱毛症を治療するためのビタミンd3およびその類似体 |
WO2014194133A1 (fr) | 2013-05-29 | 2014-12-04 | Berg Llc | Prévention ou atténuation de l'alopécie induite par la chimiothérapie au moyen de vitamine d |
CN114044788A (zh) * | 2021-08-12 | 2022-02-15 | 甘肃皓天医药科技有限责任公司 | 一种氟骨化醇cd环的制备方法及其应用 |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA2166898C (fr) | 1993-07-09 | 2004-09-07 | Roger Bouillon | Nouveaux analogues structurels de la vitamine d |
PL174912B1 (pl) | 1994-01-24 | 1998-10-30 | Inst Farmaceutyczny | Nowe związki farmakologicznie czynne z grupy witamin D i sposób ich otrzymywania |
US5461116A (en) | 1994-11-10 | 1995-10-24 | Shell Oil Company | Core functionalized star block copolymers |
EP0983221B1 (fr) * | 1997-05-23 | 2002-04-03 | Basilea Pharmaceutica AG | Derives cyclohexanediol |
-
1999
- 1999-02-18 US US09/252,508 patent/US6184422B1/en not_active Expired - Lifetime
- 1999-02-20 AU AU26246/99A patent/AU751241B2/en not_active Ceased
- 1999-02-20 EP EP99906250A patent/EP1056716B1/fr not_active Expired - Lifetime
- 1999-02-20 PT PT99906250T patent/PT1056716E/pt unknown
- 1999-02-20 JP JP2000533405A patent/JP3507435B2/ja not_active Expired - Fee Related
- 1999-02-20 AT AT99906250T patent/ATE229503T1/de not_active IP Right Cessation
- 1999-02-20 DK DK99906250T patent/DK1056716T3/da active
- 1999-02-20 CN CNB998033146A patent/CN1133621C/zh not_active Expired - Lifetime
- 1999-02-20 BR BR9908315-9A patent/BR9908315A/pt not_active IP Right Cessation
- 1999-02-20 TR TR2000/02477T patent/TR200002477T2/xx unknown
- 1999-02-20 ES ES99906250T patent/ES2188134T3/es not_active Expired - Lifetime
- 1999-02-20 KR KR1020007009419A patent/KR20010041313A/ko active IP Right Grant
- 1999-02-20 DE DE69904442T patent/DE69904442T2/de not_active Expired - Lifetime
- 1999-02-20 CA CA002320180A patent/CA2320180C/fr not_active Expired - Fee Related
- 1999-02-20 WO PCT/EP1999/001118 patent/WO1999043646A1/fr active IP Right Grant
- 1999-02-22 MA MA25470A patent/MA26609A1/fr unknown
- 1999-02-22 PE PE1999000151A patent/PE20000267A1/es not_active Application Discontinuation
- 1999-02-24 MY MYPI99000648A patent/MY133520A/en unknown
- 1999-02-24 CO CO99011496A patent/CO4980898A1/es unknown
- 1999-02-24 AR ARP990100773A patent/AR018120A1/es not_active Application Discontinuation
- 1999-02-25 ZA ZA9901550A patent/ZA991550B/xx unknown
Also Published As
Publication number | Publication date |
---|---|
KR20010041313A (ko) | 2001-05-15 |
MY133520A (en) | 2007-11-30 |
PE20000267A1 (es) | 2000-04-10 |
TR200002477T2 (tr) | 2001-03-21 |
JP2002504537A (ja) | 2002-02-12 |
CA2320180A1 (fr) | 1999-09-02 |
DE69904442T2 (de) | 2003-09-25 |
CN1291974A (zh) | 2001-04-18 |
EP1056716B1 (fr) | 2002-12-11 |
BR9908315A (pt) | 2000-11-07 |
AU751241B2 (en) | 2002-08-08 |
MA26609A1 (fr) | 2004-12-20 |
DK1056716T3 (da) | 2003-04-07 |
WO1999043646A1 (fr) | 1999-09-02 |
CN1133621C (zh) | 2004-01-07 |
DE69904442D1 (en) | 2003-01-23 |
EP1056716A1 (fr) | 2000-12-06 |
JP3507435B2 (ja) | 2004-03-15 |
PT1056716E (pt) | 2003-04-30 |
AU2624699A (en) | 1999-09-15 |
CO4980898A1 (es) | 2000-11-27 |
AR018120A1 (es) | 2001-10-31 |
ATE229503T1 (de) | 2002-12-15 |
US6184422B1 (en) | 2001-02-06 |
ES2188134T3 (es) | 2003-06-16 |
ZA991550B (en) | 1999-08-26 |
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